US10351793B2 - Refrigerator oil and working fluid composition for refrigerators - Google Patents

Refrigerator oil and working fluid composition for refrigerators Download PDF

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US10351793B2
US10351793B2 US15/550,177 US201615550177A US10351793B2 US 10351793 B2 US10351793 B2 US 10351793B2 US 201615550177 A US201615550177 A US 201615550177A US 10351793 B2 US10351793 B2 US 10351793B2
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refrigerating machine
mass
acid
ester
working fluid
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US20180023025A1 (en
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Hitoshi Takahashi
Takeshi Okido
Souichirou Konno
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Eneos Corp
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JXTG Nippon Oil and Energy Corp
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    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M169/00Lubricating compositions characterised by containing as components a mixture of at least two types of ingredient selected from base-materials, thickeners or additives, covered by the preceding groups, each of these compounds being essential
    • C10M169/04Mixtures of base-materials and additives
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09KMATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K5/00Heat-transfer, heat-exchange or heat-storage materials, e.g. refrigerants; Materials for the production of heat or cold by chemical reactions other than by combustion
    • C09K5/02Materials undergoing a change of physical state when used
    • C09K5/04Materials undergoing a change of physical state when used the change of state being from liquid to vapour or vice versa
    • C09K5/041Materials undergoing a change of physical state when used the change of state being from liquid to vapour or vice versa for compression-type refrigeration systems
    • C09K5/044Materials undergoing a change of physical state when used the change of state being from liquid to vapour or vice versa for compression-type refrigeration systems comprising halogenated compounds
    • C09K5/045Materials undergoing a change of physical state when used the change of state being from liquid to vapour or vice versa for compression-type refrigeration systems comprising halogenated compounds containing only fluorine as halogen
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M105/00Lubricating compositions characterised by the base-material being a non-macromolecular organic compound
    • C10M105/08Lubricating compositions characterised by the base-material being a non-macromolecular organic compound containing oxygen
    • C10M105/32Esters
    • C10M105/34Esters of monocarboxylic acids
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M105/00Lubricating compositions characterised by the base-material being a non-macromolecular organic compound
    • C10M105/08Lubricating compositions characterised by the base-material being a non-macromolecular organic compound containing oxygen
    • C10M105/32Esters
    • C10M105/38Esters of polyhydroxy compounds
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M129/00Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing oxygen
    • C10M129/02Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing oxygen having a carbon chain of less than 30 atoms
    • C10M129/16Ethers
    • C10M129/18Epoxides
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M129/00Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing oxygen
    • C10M129/02Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing oxygen having a carbon chain of less than 30 atoms
    • C10M129/66Epoxidised acids or esters
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M171/00Lubricating compositions characterised by purely physical criteria, e.g. containing as base-material, thickener or additive, ingredients which are characterised exclusively by their numerically specified physical properties, i.e. containing ingredients which are physically well-defined but for which the chemical nature is either unspecified or only very vaguely indicated
    • C10M171/008Lubricant compositions compatible with refrigerants
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09KMATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K2205/00Aspects relating to compounds used in compression type refrigeration systems
    • C09K2205/10Components
    • C09K2205/12Hydrocarbons
    • C09K2205/122Halogenated hydrocarbons
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09KMATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K2205/00Aspects relating to compounds used in compression type refrigeration systems
    • C09K2205/24Only one single fluoro component present
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09KMATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K5/00Heat-transfer, heat-exchange or heat-storage materials, e.g. refrigerants; Materials for the production of heat or cold by chemical reactions other than by combustion
    • C09K5/02Materials undergoing a change of physical state when used
    • C09K5/04Materials undergoing a change of physical state when used the change of state being from liquid to vapour or vice versa
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/04Ethers; Acetals; Ortho-esters; Ortho-carbonates
    • C10M2207/042Epoxides
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/28Esters
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/28Esters
    • C10M2207/281Esters of (cyclo)aliphatic monocarboxylic acids
    • C10M2207/2815Esters of (cyclo)aliphatic monocarboxylic acids used as base material
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/28Esters
    • C10M2207/283Esters of polyhydroxy compounds
    • C10M2207/2835Esters of polyhydroxy compounds used as base material
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10NINDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2030/00Specified physical or chemical properties which is improved by the additive characterising the lubricating composition, e.g. multifunctional additives
    • C10N2030/08Resistance to extreme temperature
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10NINDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2040/00Specified use or application for which the lubricating composition is intended
    • C10N2040/30Refrigerators lubricants or compressors lubricants
    • C10N2230/08
    • C10N2240/30

Definitions

  • the present invention relates to a refrigerating machine oil and a working fluid composition for a refrigerating machine.
  • Refrigerating machines such as refrigerators, car air-conditioners, room air-conditioners, and automatic vending machines have a compressor for circulating a refrigerant in a refrigeration cycle.
  • the compressor is charged with a refrigerating machine oil for lubricating a sliding part.
  • the refrigerating machine oil is used in the refrigeration cycle in the coexistence of a refrigerant at a wide range of temperatures from low to high temperatures and, therefore, the refrigerating machine oil is required to have various properties such as: lubricity, and thermal and chemical stability, in the presence of the refrigerant; compatibility with the refrigerant; and low-temperature properties.
  • Such properties of a refrigerating machine oil may show unpredictable behaviors depending on the kind of the coexisting refrigerant; thus, development of a refrigerating machine oil is necessary for each refrigerant.
  • Patent Literature 1 discloses a polyolester oil and polyvinyl ether oil having predetermined properties as refrigerating machine oils that improve wear resistance in the presence of a difluoromethane refrigerant.
  • Patent Literature 1 International Publication No. WO 2012/086518
  • An object of the present invention is to provide a refrigerating machine oil and a working fluid composition for a refrigerating machine that can exhibit both good low-temperature deposition property and high thermal and chemical stability.
  • the present inventors first studied the factors influencing the low-temperature deposition property and thermal and chemical stability of a refrigerating machine oil. As a result, the present inventors have found that an acid scavenger used for improvement in thermal and chemical stability can influence the low-temperature deposition property, and that the thermal and chemical stability as well as the low-temperature deposition property can change depending on the types of the base oil and acid scavenger.
  • the present invention provides a refrigerating machine oil comprising: a base oil comprising an ester of dipentaerythritol with 2-methylbutanoic acid and n-pentanoic acid; and at least one epoxy compound selected from the group consisting of a glycidyl ester compound and a glycidyl ether compound, the refrigerating machine oil being used with a difluoromethane refrigerant.
  • a ratio of the ester in the base oil be 30% by mass or more and 100% by mass or less.
  • a content of the epoxy compound be 0.01% by mass or more and 5.0% by mass or less based on a total amount of the refrigerating machine oil.
  • the present invention also provides a working fluid composition for a refrigerating machine comprising the above refrigerating machine oil and a difluoromethane refrigerant.
  • a refrigerating machine oil and a working fluid composition for a refrigerating machine that can exhibit both good low-temperature deposition property and high thermal and chemical stability can be provided.
  • the refrigerating machine oil comprises: a base oil containing an ester of dipentaerythritol with 2-methylbutanoic acid and n-pentanoic acid; and at least one epoxy compound selected from the group consisting of a glycidyl ester compound and a glycidyl ether compound.
  • the base oil contains an ester of dipentaerythritol with 2-methylbutanoic acid and n-pentanoic acid.
  • the ester can be obtained, for example, by reacting dipentaerythritol with an acid mixture of 2-methylbutanoic acid and n-pentanoic acid.
  • the molar ratio between 2-methylbutanoic acid and n-pentanoic acid (2-methylbutanoic acid:n-pentanoic acid) in fatty acids constituting the ester is preferably from 9:1 to 1:9, more preferably from 8:2 to 2:8, and further preferably from 7:3 to 3:7, from the viewpoint of more superior low-temperature deposition property.
  • the base oil may further contain another base oil in addition to the ester of dipentaerythritol with 2-methylbutanoic acid and n-pentanoic acid.
  • the other base oil include: hydrocarbon oils such as mineral oils, olefin polymers, naphthalene compounds, and alkylbenzenes; and oxygen-containing synthetic oils such as esters other than the above ester, polyglycols, polyvinyl ethers, ketones, polyphenyl ethers, silicones, polysiloxanes, and perfluoroethers.
  • the oxygen-containing synthetic oil is preferably an ester other than the above ester, a polyglycol, and a polyvinyl ether, and is more preferably an ester other than the above ester.
  • the ester other than the above ester is preferably an ester of a polyhydric alcohol and a fatty acid.
  • the polyhydric alcohol constituting the ester is, for example, a polyhydric alcohol having 2 to 6 hydroxy groups, and is preferably a hindered alcohol such as neopentyl glycol, trimethylolethane, trimethylolpropane, trimethylolbutane, di-(trimethylolpropane), tri-(trimethylolpropane), pentaerythritol, or dipentaerythritol.
  • the polyhydric alcohol is more preferably pentaerythritol, because it is especially superior in compatibility with a refrigerant and hydrolysis stability.
  • the fatty acid constituting the ester is preferably a saturated fatty acid.
  • the number of carbon atoms of the fatty acid is preferably from 4 to 20, more preferably from 4 to 18, further preferably from 4 to 9, and especially preferably from 5 to 9.
  • Examples of C4 to C20 fatty acids include butanoic acid, pentanoic acid, hexanoic acid, heptanoic acid, octanoic acid, nonanoic acid, decanoic acid, undecanoic acid, dodecanoic acid, tridecanoic acid, tetradecanoic acid, pentadecanoic acid, hexadecanoic acid, heptadecanoic acid, octadecanoic acid, nonadecanoic acid, and icosanoic acid.
  • C4 to C20 fatty acids may be linear or branched and are preferably branched.
  • the C4 to C20 branched fatty acid is preferably a fatty acid branched at a position and/or ⁇ position, and is more preferably 2-methylpropanoic acid, 2-methylbutanoic acid, 2-methylpentanoic acid, 2-methylhexanoic acid, 2-ethylpentanoic acid, 2-methylheptanoic acid, 2-ethylhexanoic acid, 3,5,5-trimethylhexanoic acid, or 2-ethylhexadecanoic acid, and is further preferably 2-ethylhexanoic acid or 3,5,5-trimethylhexanoic acid.
  • the ratio of the ester of dipentaerythritol with 2-methylbutanoic acid and n-pentanoic acid in the base oil is preferably 10% by mass or more, more preferably 20% by mass or more, further preferably 30% by mass or more, especially preferably 40% by mass or more, and most preferably 50% by mass or more from the viewpoint of more superior low-temperature deposition property, and may be 100% by mass or less.
  • the ratio of the ester of dipentaerythritol with 2-methylbutanoic acid and n-pentanoic acid in the base oil means the ratio of the total amount of an ester in which both 2-methylbutanoic acid and n-pentanoic acid are bonded to one dipentaerythritol molecule and an ester in which either 2-methylbutanoic acid or n-pentanoic acid is bonded to one dipentaerythritol molecule to the total amount of the base oil.
  • the content of the base oil may be preferably 50% by mass or more, more preferably 70% by mass or more, and further preferably 90% by mass or more based on the total amount of the refrigerating machine oil.
  • the kinematic viscosity of the base oil at 40° C. may be preferably 3 mm 2 /s or more, more preferably 4 mm 2 /s or more, and further preferably 5 mm 2 /s or more, and may be preferably 1000 mm 2 /s or less, more preferably 500 mm 2 /s or less, and further preferably 400 mm 2 /s or less.
  • the kinematic viscosity of the base oil at 100° C. may be preferably 1 mm 2 /s or more and more preferably 2 mm 2 /s or more, and may be preferably 100 mm 2 /s or less and more preferably 50 mm 2 /s or less.
  • a kinematic viscosity as used herein means a kinematic viscosity measured according to JIS K 2283: 2000.
  • the refrigerating machine oil comprises one or more epoxy compounds selected from glycidyl ester compounds and glycidyl ether compounds.
  • An example of the glycidyl ester compound (which may be referred to as “glycidyl ester type epoxy compound”) is a compound represented by the following formula (1).
  • An example of the glycidyl ether compound (which may be referred to as “glycidyl ether type epoxy compound”) is a compound represented by the following formula (2).
  • R 1 represents an aryl group, an alkyl group, or an alkenyl group.
  • R 2 represents an aryl group or an alkyl group.
  • the number of carbon atoms of the aryl group, alkyl group, and alkenyl group represented by R 1 and the number of carbon atoms of the aryl group and alkyl group represented by R 2 are preferably from 5 to 18.
  • the number of carbon atoms is 5 or more, sufficient stability of the epoxy compounds is ensured, and decomposition prior to reaction with water, a fatty acid, or an oxidatively degraded product, or self-polymerization in which the epoxy compounds polymerize with each other, can be prevented so that the desired functions can easily be obtained.
  • the solubility in a refrigerant is maintained so well that the Presence of defects such as poor cooling due to deposition in a refrigerating apparatus can be reduced.
  • Preferred as the glycidyl ester type epoxy compound represented by the formula (1) are glycidyl benzoate, glycidyl neodecanoate, glycidyl 2,2-dimethyloctanoate, glycidyl acrylate, and glycidyl methacrylate.
  • Preferred as the glycidyl ether type epoxy compound represented by the formula (2) are n-butylphenyl glycidyl ether, i-butylphenyl glycidyl ether, sec-butylphenyl glycidyl ether, tert-butylphenyl glycidyl ether, pentylphenyl glycidyl ether, hexylphenyl glycidyl ether, heptylphenyl glycidyl ether, octylphenyl glycidyl ether, nonylphenyl glycidyl ether, decylphenyl glycidyl ether, decyl glycidyl ether, undecyl glycidyl ether, dodecyl glycidyl ether, tridecyl glycidyl ether, tetradecyl
  • the glycidyl ether type epoxy compound may be, for example, neopentyl glycol diglycidyl ether, trimethylolpropane triglycidyl ether, pentaerythritol tetraglycidyl ether, 1,6-hexanediol diglycidyl ether, sorbitol polyglycidyl ether, polyalkylene glycol monoglycidyl ether, and polyalkylene glycol diglycidyl ether, rather than the epoxy compound represented by the formula (2).
  • the content of the epoxy compounds is preferably 0.01% by mass or more, more preferably 0.05% by mass or more, and further preferably 0.1% by mass or more based on the total amount of the refrigerating machine oil from the viewpoint of stability, and is preferably 10.0% by mass or less, more preferably 7.0% by mass or less, and further preferably 5.0% by mass or less based on the total amount of the refrigerating machine oil from the viewpoint of lubricity.
  • the content of the epoxy compounds is preferably from 0.01 to 10.0% by mass, from 0.01 to 7.0% by mass, from 0.01 to 5.0% by mass, from 0.05 to 10.0% by mass, from 0.05 to 7.0% by mass, from 0.05 to 5.0% by mass, from 0.1 to 10.0% by mass, from 0.1 to 7.0% by mass, or from 0.1 to 5.0% by mass from the viewpoint of good balance between stability and lubricity.
  • the refrigerating machine oil may further contain another additive in addition to the glycidyl ester compound and glycidyl ether compound.
  • the other additive include: phenolic antioxidants such as 2,6-di-tert-butyl-p-cresol and bisphenol A; amine antioxidants such as phenyl- ⁇ -naphthylamine and N,N-di(2-naphthyl)-p-phenylenediamine; extreme-pressure agents such as chlorinated paraffin, phosphorus compounds, and sulfur compounds; oily agents such as fatty acids; antifoaming agents such as those based on silicones; metal deactivators such as benzotriazole; antiwear agents; viscosity index improving agents; pour-point depressants; and detergent dispersants.
  • the content of these additives may be preferably 10% by mass or less and more preferably 5% by mass or less based on the total amount of the refrigerating machine oil.
  • the kinematic viscosity of the refrigerating machine oil at 40° C. is preferably 3 mm 2 /s or more, more preferably 4 mm 2 /s or more, and further preferably 5 mm 2 /s or more from the viewpoint of superior lubricity.
  • the kinematic viscosity of the refrigerating machine oil at 40° C. is preferably 1000 mm 2 /s or less, more preferably 500 mm 2 /s or less, and further preferably 400 mm 2 /s or less from the viewpoint of superior oil return performance.
  • mm 2 /s is preferably from 3 to 1000 mm 2 /s, from 3 to 500 mm 2 /s, from 3 to 400 mm 2 /s, from 4 to 1000 mm 2 /s, from 4 to 500 mm 2 /s, from 4 to 400 mm 2 /s, from 5 to 1000 mm 2 /s, from 5 to 500 mm 2 /s, or from 5 to 400 mm 2 /s from the viewpoint of good balance between lubricity and oil return performance.
  • the kinematic viscosity of the refrigerating machine oil at 100° C. is preferably 1 mm 2 /s or more and more preferably 2 mm 2 /s or more from the viewpoint of superior lubricity.
  • the kinematic viscosity of the refrigerating machine oil at 100° C. is preferably 100 mm 2 /s or less and more preferably 50 mm 2 /s or less from the viewpoint of superior oil return performance.
  • the kinematic viscosity of the refrigerating machine oil at 100° C. is preferably from 1 to 100 mm 2 /s, from 1 to 50 mm 2 /s, from 2 to 100 mm 2 /s, or from 2 to 50 mm 2 /s from the viewpoint of good balance between lubricity and oil return performance.
  • the volume resistivity of a refrigerating machine oil is preferably 1.0 ⁇ 10 10 ⁇ cm or more, more preferably 1.0 ⁇ 10 11 ⁇ cm or more, and further preferably 1.0 ⁇ 10 12 ⁇ cm or more. Especially, when a refrigerating machine oil is used in a closed refrigerating machine, a high electrical insulation tends to be required.
  • a volume resistivity as used herein means a volume resistivity measured at 25° C. according to JIS C2101: 1999.
  • the moisture content of the refrigerating machine oil is preferably 300 ppm or less, more preferably 200 ppm or less, and further preferably 100 ppm or less based on the total amount of the refrigerating machine oil.
  • a refrigerating machine oil is used in a closed refrigerating machine, a low moisture content is required from the viewpoints of the thermal and chemical stability of a refrigerating machine oil, or influence on electrical insulation.
  • the acid value of the refrigerating machine oil is preferably 0.1 mg KOH/g or less and more preferably 0.05 mg KOH/g or less.
  • the hydroxyl value of the refrigerating machine oil is preferably 5.0 mg KOH/g or less and more preferably 2.0 mg KOH/g or less.
  • An acid value as used herein means an acid value measured according to JIS K 2501: 2003.
  • a hydroxyl value as used herein means a hydroxyl value measured according to JIS K 0070-1992.
  • the ash content of the refrigerating machine oil is preferably 100 ppm or less and more preferably 50 ppm or less from the viewpoint of enhancing the thermal and chemical stability of the refrigerating machine oil to prevent formation of sludge or the like.
  • An ash content as used herein means an ash measured according to JIS K 2272: 1998.
  • the pour point of a refrigerating machine oil may be preferably ⁇ 10° C. or less, more preferably ⁇ 20° C. or less, and further preferably ⁇ 30° C. or less.
  • a pour point as used herein means a pour point measured according to JIS K2269:1987.
  • the refrigerating machine oil according to the present embodiment is used in combination with a difluoromethane refrigerant (HFC-32).
  • the working fluid composition for a refrigerating machine according to the present embodiment contains the above refrigerating machine oil and a difluoromethane refrigerant.
  • a composition containing an ester of dipentaerythritol with 2-methylbutanoic acid and n-pentanoic acid and at least one epoxy compound selected from the group consisting of a glycidyl ester compound and a glycidyl ether compound is favorably utilized as a constituent of a refrigerating machine oil to be used in combination with a difluoromethane refrigerant or as a constituent of a working fluid composition for a refrigerating machine containing a refrigerating machine oil and a difluoromethane refrigerant.
  • a composition containing an ester of dipentaerythritol with 2-methylbutanoic acid and n-pentanoic acid and at least one epoxy compound selected from the group consisting of a glycidyl ester compound and a glycidyl ether compound is favorably utilized in production of a refrigerating machine oil to be used in combination with a difluoromethane refrigerant or in production of a working fluid composition for a refrigerating machine containing a refrigerating machine oil and a difluoromethane refrigerant.
  • the refrigerant may consist of difluoromethane and may contain another refrigerant in addition to difluoromethane.
  • the other refrigerant include: saturated hydrofluorocarbon refrigerants other than difluoromethane; unsaturated hydrofluorocarbon refrigerants; fluorine-containing ether refrigerants such as perfluoroethers; bis(trifluoromethyl)sulfide refrigerants; trifluoroiodomethane refrigerants; and natural refrigerants such as dimethyl ether, carbon dioxide, ammonia, and hydrocarbons.
  • the saturated hydrofluorocarbon refrigerants other than difluoromethane include pentafluoroethane (HFC-125), 1,1,2,2-tetrafluoroethane (HFC-134), 1,1,1,2-tetrafluoro ethane (HFC-134a), 1,1-difluoroethane (HFC-152a), fluoroethane (HFC-161), 1,1,1,2,3,3,3-heptafluoropropane (HFC-227ea), 1,1,1,2,3,3-hexafluoropropane (HFC-236ea), 1,1,1,3,3,3-hexafluoropropane (HFC-236fa), 1,1,1,3,3-pentafluoropropane (HFC-245fa), and 1,1,1,3,3-pentafluorobutane (HFC-365mfc).
  • 1,1,1,2-tetrafluoroethane (HFC-134a) is preferable from the viewpoint
  • Examples of an unsaturated hydrofluorocarbon refrigerant include 1,2,3,3,3-pentafluoropropene (HFO-1225ye), 1,3,3,3-tetrafluoropropene (HFO-1234ze), 2,3,3,3-tetrafluoropropene (HFO-1234yf), 1,2,3,3-tetrafluoropropene (HFO-1234ye), and 3,3,3-trifluoropropene (HFO-1243zf).
  • 1,3,3,3-tetrafluoropropene (HFO-1234ze) and 2,3,3,3-tetrafluoropropene (HFO-1234yf) are preferred, and 2,3,3,3-tetrafluoropropene (HFO-1234yf) is more preferred from the viewpoint of the stability of the refrigerating machine oil in a refrigerant atmosphere and from the viewpoint of reduction of GWP.
  • the content of difluoromethane may be preferably 5% by mass or more, more preferably 10% by mass or more, and further preferably 20% by mass or more based on the total amount of the refrigerant.
  • the content of a refrigerating machine oil in a working fluid composition for a refrigerating machine may be preferably 1 part by mass or more based on 100 parts by mass of a refrigerant, and more preferably 2 parts by mass or more; and may be preferably 500 parts by mass or less, and more preferably 400 parts by mass.
  • a refrigerating machine oil and a working fluid composition for a refrigerating machine are used advantageously in an air-conditioner, a refrigerator, or an open- or closed type car air-conditioner provided with a reciprocal or rotary closed type compressor.
  • a refrigerating machine oil and a working fluid composition for a refrigerating machine are used advantageously in a cooling device, etc. such as a dehumidifier, a water heater, a freezer, a refrigerator/freezer storehouse, an automatic vending machine, a showcase, and a chemical plant.
  • a refrigerating machine oil and a working fluid composition for a refrigerating machine are also used advantageously in a refrigerating machine provided with a centrifugal compressor.
  • Refrigerating machine oils with compositions shown in Tables 2 and 3 were prepared using polyhydric alcohol fatty acid esters (base oils) shown in Table 1 and additives listed below.
  • base oils polyhydric alcohol fatty acid esters
  • Table 1 the composition of each base oil is expressed by % by mass based on the total amount of the base oil
  • composition of each refrigerating machine oil is expressed by % by mass based on the total amount of the refrigerating machine oil.
  • a stability test was conducted according to JIS K2211: 2009 (Autoclave test). That is, 40 g of each refrigerating machine oil conditioned to a moisture content of 500 ppm was weighed into an autoclave, in which a catalyst (iron wire, copper wire, and aluminum wire, each having an outer diameter of 1.6 mm and a length of 50 mm) and 10 g of a difluoromethane (R32) refrigerant were placed and which was closed and then heated at 180° C. for 150 hours. After that, the acid value (JIS C 2101) of the refrigerating machine oil was measured.
  • a catalyst iron wire, copper wire, and aluminum wire, each having an outer diameter of 1.6 mm and a length of 50 mm
  • R32 difluoromethane
  • Example 1 Example 2
  • Example 3 Example 4
  • Example 5 Composition of A1 100 — 100 — — base oil
  • A3 — — — — 50 Composition of Base oil remainder remainder remainder remainder remainder refrigerating machine
  • B1 0.1 — 3.0 — — oil
  • Stability test Acid value 0.01 0.01 0.01 0.01 0.04 (mgKOH/g)
  • Example 2 Composition of A1 — 100 — 100 100 base oil A2 30 — 100 — — (% by mass) A3 70 — — — — — Composition of Base oil remainder remainder remainder remainder refrigerating machine B1 — — 0.1 — — oil B2 2.0 0.1 — — — (% by mass) B3 — — — 3.0 0.5 Stability test Acid value 0.06 0.01 0.01 0.08 0.09 (mgKOH/g) Low-temperature Presence or Absence Absence Absence Presence Presence deposition property Absence of after stability test deposition
  • Example 7 Composition of A1 — 100 — — — base oil A2 — — 100 — — (% by mass) A3 100 — — 100 100 Composition of Base oil remainder remainder remainder remainder remainder refrigerating machine B1 — — — 0.5 — oil B2 — — — — 0.5 (% by mass) B3 0.5 — — — — Stability test Acid value 0.13 0.19 0.15 0.28 0.34 (mgKOH/g) Low-temperature Presence or Presence Absence Absence Absence Absence deposition property Absence of after stability test deposition

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JP2017075278A (ja) * 2015-10-16 2017-04-20 出光興産株式会社 冷凍機油、冷凍機用組成物、及び冷凍機
CN109852348B (zh) * 2019-01-10 2020-10-23 珠海格力电器股份有限公司 环保混合工质
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